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1-Pyrroline-5-carboxylate dehydrogenase

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1-pyrroline-5-carboxylate dehydrogenase
Identifiers
EC no.1.2.1.88
CAS no.9054-82-4
Databases
BRENDAenzyme data
ExPASyNiceZyme view
KEGGenzyme entry
MetaCycmetabolic pathway
Rheareactions
PDB structuresRCSB PDB PDBe PDBsum
Gene OntologyAmiGO / QuickGO
Search
PMCarticles
PubMedarticles
NCBIproteins

In enzymology, 1-pyrroline-5-carboxylate dehydrogenase (EC 1.2.1.88) is an enzyme that catalyzes the chemical reaction

 
 
 
Reversible left-right reaction arrow
 
 
 
+ NAD+
 
 
H2O
H+
Reversible left-right reaction arrow with minor forward substrate(s) from top left, minor forward product(s) to top right, minor reverse substrate(s) from bottom right and minor reverse product(s) to bottom left
H2O
H+
 
+ NADH
 

The three substrates of this enzyme are (S)-1-pyrroline-5-carboxylate, nicotinamide adenine dinucleotide (NAD+), and water. The starting material is in chemical equilibrium with L-glutamate-5-semialdehyde, which is oxidised to L-glutamic acid, giving reduced NADH, and a proton.[1][2][3]

This enzyme belongs to the family of oxidoreductases, specifically those acting on the CH-NH group of donors with NAD+ or NADP+ as acceptor. The systematic name of this enzyme class is (S)-1-pyrroline-5-carboxylate:NAD+ oxidoreductase. Other names in common use include delta-1-pyrroline-5-carboxylate dehydrogenase, 1-pyrroline dehydrogenase, pyrroline-5-carboxylate dehydrogenase, pyrroline-5-carboxylic acid dehydrogenase, L-pyrroline-5-carboxylate-NAD+ oxidoreductase, and 1-pyrroline-5-carboxylate:NAD+ oxidoreductase. This enzyme participates in glutamate metabolism and arginine and proline metabolism.

Structural studies

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As of late 2007, 14 structures have been solved for this class of enzymes, with PDB accession codes PDB: 2BHP​, PDB: 2BHQ​, PDB: 2BJA​, PDB: 2BJK​, PDB: 2EHQ​, PDB: 2EHU​, PDB: 2EII​, PDB: 2EIT​, PDB: 2EIW​, PDB: 2EJ6​, PDB: 2EJD​, PDB: 2EJL​, PDB: 2IY6​, and PDB: 2J40​.

Human gene

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In human, the protein is encoded by ALDH4A1 gene.

References

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  1. ↑ Enzyme 1.2.1.88 at KEGG Pathway Database.
  2. ↑ Adams E, Goldstone A (December 1960). "Hydroxyproline metabolism. IV. Enzymatic synthesis of gamma-hydroxyglutamate from Delta 1-pyrroline-3-hydroxy-5-carboxylate". The Journal of Biological Chemistry. 235 (12): 3504–12. doi:10.1016/S0021-9258(18)64498-9. PMID 13681370.
  3. ↑ Strecker HJ (1960). "The interconversion of glutamic acid proline. III Delta1-Pyrroline-5-carboxylic acid dehydrogenase". J. Biol. Chem. 235: 3218–3223. doi:10.1016/S0021-9258(20)81340-4.